Canonical Allele Identifier: PA2827678301
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 945673
ClinVar RCV Id: RCV001216371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Met76Val
CA399506051
NM_001352774.2:c.226A>G